1.
Batzoglou S, Berger B, Mesirov J, Lander ES. Sequencing a genome by walking with clone-end sequences: a mathematical analysis. Genome Res. 1999;9(12):1163-74.
Eric Lander
1.
Wyrick JJ, Holstege FC, Jennings EG, et al. Chromosomal landscape of nucleosome-dependent gene expression and silencing in yeast. Nature. 1999;402(6760):418-21. doi:10.1038/46567.
1.
Madhani HD, Galitski T, Lander ES, Fink GR. Effectors of a developmental mitogen-activated protein kinase cascade revealed by expression signatures of signaling mutants. Proc Natl Acad Sci U S A. 1999;96(22):12530-5.
1.
Hästbacka J, Kerrebrock A, Mokkala K, et al. Identification of the Finnish founder mutation for diastrophic dysplasia (DTD). Eur J Hum Genet. 1999;7(6):664-70. doi:10.1038/sj.ejhg.5200361.
1.
Pachter L, Batzoglou S, Spitkovsky VI, et al. A dictionary-based approach for gene annotation. J Comput Biol. 1999;6(3-4):419-30. doi:10.1089/106652799318364.
1.
Klaff LS, Koike G, Jiang J, et al. BB rat diabetes susceptibility and body weight regulation genes colocalize on chromosome 2. Mamm Genome. 1999;10(9):883-7.
1.
Sidow A, Bulotsky MS, Kerrebrock AW, et al. A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant. Nat Genet. 1999;23(1):104-7. doi:10.1038/12709.
1.
Van Etten WJ, Steen RG, Nguyen H, et al. Radiation hybrid map of the mouse genome. Nat Genet. 1999;22(4):384-7. doi:10.1038/11962.
1.
Nusbaum C, Slonim DK, Harris KL, et al. A YAC-based physical map of the mouse genome. Nat Genet. 1999;22(4):388-93. doi:10.1038/11967.
1.
Pfeifer D, Kist R, Dewar K, et al. Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region. Am J Hum Genet. 1999;65(1):111-24. doi:10.1086/302455.